Shandong Anshun Pharmaceutical Co., Ltd.

FDA inspection history in Dezhou City, China, 2020

1
Form 483

Every document, by year

  • Form 483

2020: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2020One Form 483, at Dezhou City, China.

Cited most

Across all Shandong Anshun Pharmaceutical Co. observations on file

The complete Shandong Anshun Pharmaceutical Co. file.

All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.

$99

The documents one by one, while the file is prepared

See the documents

Sites

Documents

1 on file, newest first
DateDocumentPrice
2020-11-20483 Form 483$99

Investigators on these documents

Marcus A. Ray (1)

FEI number 3015326904 · most recent document Nov 20, 2020

About Shandong Anshun Pharmaceutical Co., Ltd.

How many FDA Form 483s has Shandong Anshun Pharmaceutical Co., Ltd. received?

FDA Intel has 1 Form 483 on file for Shandong Anshun Pharmaceutical Co., Ltd.; the most recent is dated Nov 20, 2020.

When was Shandong Anshun Pharmaceutical Co., Ltd. last inspected by FDA?

The most recent FDA inspection document on file for Shandong Anshun Pharmaceutical Co., Ltd. is a Form 483 dated Nov 20, 2020, for the site in Dezhou City, China.

What did FDA cite at Shandong Anshun Pharmaceutical Co., Ltd.?

The regulations cited most in the observations on file for Shandong Anshun Pharmaceutical Co., Ltd. are 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.25 (Personnel qualifications), 1 time.